Canonical Allele Identifier: CA2173248601

Gene: STRC CKMT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43601546C= , CM000677.2:g.43601546C=	GRCh38
NC_000015.9:g.43893744C= , CM000677.1:g.43893744C=	GRCh37
NC_000015.8:g.41681036C=	NCBI36
NG_011636.1:g.22255G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4551G= (STRC) MANE Select	ENSP00000401513.2:p.Trp1517=
ENST00000411560.1:n.142+2013C= (CKMT1B)
ENST00000428650.5:c.*1584G= (STRC)	ENSP00000415991.1:n.*1584G=
ENST00000440125.5:c.*2343G= (STRC)	ENSP00000394866.1:n.*2343G=
ENST00000448437.6:n.1671G= (STRC)
ENST00000450892.6:c.4551G= (STRC)	ENSP00000401513.2:p.Trp1517=
ENST00000460952.1:n.130G= (STRC)
ENST00000471703.5:n.2505G= (STRC)
ENST00000485556.5:n.3406G= (STRC)
ENST00000493750.1:n.347G= (STRC)
ENST00000541030.5:c.2232G= (STRC)	ENSP00000440413.1:p.Trp744=
NM_153700.2:c.4551G= (STRC) MANE Select	NP_714544.1:p.Trp1517=
XM_011521277.1:c.5040G= (STRC)	XP_011519579.1:p.Trp1680=
XM_011521278.1:c.4656G= (STRC)	XP_011519580.1:p.Trp1552=
XM_011521279.1:c.4656G= (STRC)	XP_011519581.1:p.Trp1552=